Your browser does not support javascript! Please enable it, otherwise web will not work for you.

Clinical Research Associate (part time/freelance)

  • TFS
  • Full time
  • United States
  • 27/04/2021

  • Identify, select, and monitor performance of investigational sites for clinical studies.
  • Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations and study-specific manuals and procedures.
  • Write, contribute and review of clinical protocols, amendments, informed consent forms, study guides, case report forms, IMP release package and any other clinical research related documents.
  • Track and report on progress of study including site activation, patient enrollment, monitoring visits.
  • Act as Sponsor representative for study sites during study visits
  • Oversee proper training of staff members who are working on the study
  • Responsible for TMF maintenance.
  • Contribution in all other study activities as required


  • Education: Degree in Health Sciences, preferably Pharmacy, but also Chemistry, Biology, Biochemistry, Veterinary or similar.
  • Languages: Fluent Spanish and English, knowledge of other languages will be an asset.
  • Experience (years/area): +2 years of experience as a Clinical Research Associate.

About TFS

We believe that a company with ethical and transparent values has a better chance of attracting skilled employees and building long-term relationships.

Similar positions

Property Researcher - Remote

  • PropLogix
  • United States

Real Estate Property Researcher - Remote

  • PropLogix
  • United States

UX Researcher (Full Time, Remote)

  • Hike
  • India

Clinical Research Associate

  • TFS
  • United States

Clinical Research Associate, home or office based

  • TFS
  • Italy